Organic light emitting compound and organic light emitting diode including the same

ABSTRACT

Disclosed is an organic light emitting compound represented by Formula I: 
       HAr 1 -(L) n -HAr 2   (I)
 
     Also disclosed is an organic light emitting diode including the organic light emitting compound. Particularly, the organic light emitting diode employs the organic light emitting compound as a material for electron injection and transport. The organic light emitting diode can be driven at a low voltage and has improved life characteristics compared to conventional organic light emitting diodes. Due to these advantages, the organic light emitting diode is useful in a variety of industrial applications, including displays and lighting systems.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 15/660,388 filed Jul. 26, 2017 which claims the benefit under 35 USC § 119(a) of Korean Patent Application No. 10-2016-0095499 filed on Jul. 27, 2016, Korean Patent Application No. 10-2016-0128791 filed on Oct. 6, 2016, and Korean Patent Application No. 10-2017-0085283 filed on Jul. 5, 2017, in the Korean Intellectual Property Office, the entire disclosure of which is incorporated herein by reference for all purposes.

BACKGROUND OF THE INVENTION 1. Field of the Invention

The present invention relates to an organic light emitting compound. More specifically, the present invention relates to an organic light emitting compound that has a specific structure for an electron transport layer and can be used to achieve long lifetime, low voltage and high-efficiency luminescence, and an organic light emitting diode including the organic light emitting compound.

2. Description of the Related Art

Organic light emitting diodes (OLEDs) are self-luminous display devices and have the advantage of large viewing angle. Organic light emitting diodes can be reduced in weight, thickness, and size and have short response time compared to liquid crystal display devices. Due to these advantages, the application of organic light emitting diodes to full-color displays or lighting systems is expected.

Generally, organic electroluminescence refers to the phenomenon in which electrical energy is converted into light energy using an organic material. A typical organic light emitting diode based on organic electroluminescence has a structure including an anode, a cathode, and an organic layer therebetween.

The organic layer usually consists of one or more layers, for example, a hole injecting layer, a hole transport layer, a light emitting layer, an electron transport layer, and an electron injecting layer that are composed of different materials to increase the efficiency and stability of the organic light emitting diode.

When a voltage is applied between the two electrodes of the organic light emitting diode, holes from the anode and electrons from the cathode are injected into the organic layer. As a result of recombination of the holes and the electrons, excitons are formed which return back to the ground state to emit light. Such an organic light emitting diode is known to have excellent characteristics, such as self-luminescence, high luminance, high efficiency, low driving voltage, large viewing angle, high contrast, and fast response speed.

Materials for organic layers of organic light emitting diodes can be divided into light emitting materials and charge transport materials, for example, hole injecting materials, hole transport materials, electron transport materials, and electron injecting materials, by their functions. Organic layers of organic light emitting diodes may further include one or more layers, for example, an electron blocking layer or a hole blocking layer.

Many materials for electron transport layers are known that possess an outstanding ability to transport electrons and block holes, have high luminance efficiency and can be formed into highly stable thin films. For example, Korean Patent Publication No. 10-2012-0104204 (Sep. 20, 2012) describes an organic compound in which a pyridoindole derivative is bonded to a substituted anthracene ring structures. Further, Japanese Patent Publication No. 2010-168363 (Aug. 5, 2010) describes an anthracene derivative having a pyridylnaphthyl group that is excellent in terms of external quantum efficiency and driving voltage.

Despite numerous attempts to develop methods for fabricating organic light emitting diodes with efficient luminescent properties in the prior art, including the above patent publications, there is still a continued need to develop organic light emitting diodes with long lifetime, low voltage, and high efficiency.

SUMMARY OF THE INVENTION

Therefore, the present invention has been made in an effort to solve the above problems and is directed to providing an organic light emitting compound having a specific structure that can be introduced into an electron transport layer to fabricate an organic light emitting diode with long lifetime, low voltage, and high efficiency.

The present invention is also directed to providing an organic light emitting diode that employs the organic light emitting compound as a light emitting material to achieve low driving voltage, high efficiency, and long lifetime.

One aspect of the present invention provides an organic light emitting compound represented by Formula I:

HAr₁-(L)_(n)-HAr₂  (I)

The structure and specific substituents of the compound of Formula 1 are described below.

A further aspect of the present invention provides an organic light emitting diode including the organic light emitting compound.

The organic light emitting diode of the present invention employs the organic light emitting compound, particularly, as a material for electron injection and transport. The organic light emitting diode of the present invention exhibits low driving voltage, long lifetime, and high efficiency compared to conventional organic light emitting diodes. Due to these advantages, the organic light emitting diode of the present invention is useful in a variety of industrial applications, including displays and lighting systems.

DETAILED DESCRIPTION OF THE INVENTION

The present invention will now be described in more detail.

The present invention is directed to an organic light emitting compound represented by Formula I:

HAr₁-(L)_(n)-HAr₂  (I)

wherein L represents a linker and is a single bond or is selected from substituted or unsubstituted C₁-C₃₀ alkylene groups, substituted or unsubstituted C₂-C₃₀ alkenylene groups, substituted or unsubstituted C₂-C₃₀ alkynylene groups, substituted or unsubstituted C₃-C₃₀ cycloalkylene groups, substituted or unsubstituted C₂-C₃₀ heterocycloalkylene groups, substituted or unsubstituted C₆-C₃₀ arylene groups, and substituted or unsubstituted C₂-C₃₀ heteroarylene groups, n is an integer from 1 to 3, provided that when n is equal to or greater than 2, the plurality of L groups are identical to or different from each other, HAr₁ is a substituted or unsubstituted C₆-C₃₀ aryl group or a substituted or unsubstituted C₂-C₃₀ heteroaryl group, and HAr₂ is selected from the following structures A to E:

wherein X₁ is CR₁₁ or N, X₂ is CR₁₂ or N, X₃ is CR₁₃ or N, X₄ is CR₁₄ or N, X₅ is CR₁₅ or N, X₆ is CR₁₆ or N, X₇ is CR₁₇ or N, X₈ is CR₁₈ or N, X₉ is CR₁₉ or N, and X₁₀ is CR₂₀ or N, with the proviso that at least two of X₁ to X₄ are selected from CR₁₁ to CR₁₄, at least three of X₅ to X₁₀ are selected from CR₁₅ to CR₂₀, and one of X₁ to X₁₀ is a carbon atom linked to L, R₁, R₂, and R₁₁ to R₂₀ are identical to or different from each other and are each independently selected from a hydrogen atom, a deuterium atom, substituted or unsubstituted C₁-C₃₀ alkyl groups, substituted or unsubstituted C₂-C₃₀ alkenyl groups, substituted or unsubstituted C₂-C₃₀ alkynyl groups, substituted or unsubstituted C₃-C₃₀ cycloalkyl groups, substituted or unsubstituted C₂-C₃₀ heterocycloalkyl groups, substituted or unsubstituted C₅-C₃₀ cycloalkenyl groups, substituted or unsubstituted C₁-C₃₀ alkoxy groups, substituted or unsubstituted C₆-C₃₀ aryloxy groups, substituted or unsubstituted C₁-C₃₀ alkylthioxy groups, substituted or unsubstituted C₆-C₃₀ arylthioxy groups, substituted or unsubstituted C₁-C₃₀ alkylamine groups, substituted or unsubstituted C₆-C₃₀ arylamine groups, substituted or unsubstituted C₆-C₅₀ aryl groups, substituted or unsubstituted C₂-C₅₀ heteroaryl groups containing O, N or S as a heteroatom, substituted or unsubstituted C₁-C₂₄ alkylsilyl groups, substituted or unsubstituted C₆-C₂₄ arylsilyl groups, an amino group, a thiol group, a cyano group, a hydroxyl group, a nitro group, and halogen groups.

According to one embodiment, L may be a single bond or may be selected from the following structures 1 to 9:

wherein hydrogen or deuterium atoms are bonded to the carbon atoms of the aromatic rings.

One of R₁₁ to R₂₀ is bonded to L and the remainders of R₁₁ to R₂₀ may be hydrogen or deuterium atoms. Only one of X₁ to X₁₀ may be a nitrogen atom or none of X₁ to X₁₀ may be nitrogen atoms.

The organic light emitting compound of the present invention can be employed as an electron injecting or transport material for an organic layer of an organic light emitting diode to improve the efficiency, life characteristics, and driving voltage characteristics of the diode.

The compound of Formula I is characterized by the presence of one of Structures A to E. A more detailed description will be given of Structures A to E. Each of Structures A to E has an indenodibenzofuran structure consisting of a 6-membered aromatic ring containing X₁ to X₄, a 5-membered ring containing a carbon atom linked to R₁ and R₂, a 6-membered aromatic carbocyclic ring containing X₅ and X₁₀, X₅ and X₆ or X₉ and X₁₀, a 5-membered ring containing an oxygen atom, and a 6-membered aromatic ring containing X₆ to X₉, X₇ to X₁₀ or X₅ to X₈, which are fused to each other, and optionally including at least one nitrogen atom in the ring structure. One of X₁ to X₁₀ in these fused rings is linked to L.

HAr₁ is preferably a substituted or unsubstituted C₂-C₃₀ heteroaryl group.

According to a preferred embodiment of the present invention, HAr₁ is selected from the following structures E1 to E33:

wherein Z₁ to Z₈ are identical to or different from each other and each independently have the same meanings as R₁, R₂, and R₁₁ to R₂₀, and each of Z₁ to Z₈ and substituents thereof may optionally form an aliphatic, aromatic, heteroaliphatic or heteroaromatic fused ring with the adjacent group.

The term “substituted” in the definition of “substituted or unsubstituted” used herein refers to substitution with at least one substituent selected from the group consisting of deuterium, a cyano group, halogen groups, a hydroxyl group, a nitro group, C₁-C₂₄ alkyl groups, C₁-C₂₄ halogenated alkyl groups, C₂-C₂₄ alkenyl groups, C₂-C₂₄ alkynyl groups, C₁-C₂₄ heteroalkyl groups, C₆-C₂₄ aryl groups, C₇-C₂₄ arylalkyl groups, C₂-C₂₄ heteroaryl groups, C₂-C₂₄ heteroarylalkyl groups, C₁-C₂₄ alkoxy groups, C₁-C₂₄ alkylamino groups, C₁-C₂₄ arylamino groups, C₁-C₂₄ heteroarylamino groups, C₁-C₂₄ alkylsilyl groups, C₆-C₂₄ arylsilyl groups, and C₆-C₂₄ aryloxy groups.

In the “substituted or unsubstituted C₁-C₃₀ alkyl groups”, “substituted or unsubstituted C₆-C₃₀ aryl groups”, etc., the number of carbon atoms in each alkyl or aryl group is considered as the number of carbon atoms constituting the unsubstituted alkyl or aryl moiety and the number of carbon atoms in the substituent(s) is excluded therefrom. For example, a phenyl group substituted with a butyl group at the para-position corresponds to a C₆ aryl group substituted with a C₄ butyl group.

Specific examples of the alkyl groups used in the present invention include methyl, ethyl, propyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso-amyl, hexyl, heptyl, octyl, stearyl, trichloromethyl, and trifluoromethyl groups. At least one hydrogen atom of each alkyl group may be substituted with a deuterium atom, a halogen atom, a hydroxyl group, a nitro group, a cyano group, a trifluoromethyl group, a silyl group (herein referred to as an “alkylsilyl group”), a substituted or unsubstituted amino group (—NH₂, —NH(R) or —N(R′)(R″), in which R, R′, and R″ are each independently a C₁-C₂₄ alkyl group (the —NH(R) and —N(R′)(R″) are referred to as “alkylamino groups”), an amidino group, a hydrazine group, a hydrazone group, a carboxyl group, a sulfonic acid group, a phosphoric acid group, a C₁-C₂₄ alkyl group, a C₁-C₂₄ halogenated alkyl group, a C₂-C₂₄ alkenyl group, a C₂-C₂₄ alkynyl group, a C₁-C₂₄ heteroalkyl group, a C₅-C₂₄ aryl group, a C₆-C₂₄ arylalkyl group, a C₃-C₂₄ heteroaryl group or a C₃-C₂₄ heteroarylalkyl group.

Specific examples of the alkoxy groups used in the present invention include methoxy, ethoxy, propoxy, isobutyloxy, sec-butyloxy, pentyloxy, iso-amyloxy, and hexyloxy groups. The alkoxy groups may be substituted with the same substituents as in the alkyl groups.

Specific examples of the halogen groups used in the present invention include fluoro (F), chloro (Cl), bromo (Br), and iodo (I) groups.

The aryloxy groups used in the present invention refer to —O-aryl radicals in which the aryl group is as defined above. Specific examples of the aryloxy groups include phenoxy, naphthoxy, anthracenyloxy, phenanthrenyloxy, fluorenyloxy, and indenyloxy. At least one hydrogen atom of each aryloxy group may be substituted.

Specific examples of the silyl groups used in the present invention include trimethylsilyl, triethylsilyl, triphenylsilyl, trimethoxysilyl, dimethoxyphenylsilyl, diphenylmethylsilyl, diphenylvinylsilyl, methylcyclobutylsilyl, and dimethylfurylsilyl.

The aryl groups used in the present invention are organic radicals derived from aromatic hydrocarbons by removal of a hydrogen atom. Such aryl groups include 5- to 7-membered, preferably 5- or 6-membered single or fused ring systems. When the aryl group is substituted, the substituent may be fused with an adjacent substituent to form a ring.

Specific examples of the aryl groups include aromatic groups, such as phenyl, o-biphenyl, m-biphenyl, p-biphenyl, o-terphenyl, m-terphenyl, p-terphenyl, naphthyl, anthryl, phenanthryl, pyrenyl, indenyl, fluorenyl, tetrahydronaphthyl, perylenyl, crycenyl, naphthacenyl, and fluoranthenyl groups.

Each aryl group may also be substituted with at least one substituent. More specifically, at least one hydrogen atom of each aryl group may be substituted with a deuterium atom, a halogen atom, a hydroxyl group, a nitro group, a cyano group, a silyl group, an amino group (—NH₂, —NH(R), —N(R′)(R″) in which R, R′ and R″ are each independently a C₁-C₁₀ alkyl group (the —NH(R) and —N(R′)(R″) are referred to as “alkylamino groups”)), an amidino group, a hydrazine group, a hydrazone group, a carboxyl group, a sulfonic acid group, a phosphoric acid group, a C₁-C₂₄ alkyl group, a C₁-C₂₄ halogenated alkyl group, a C₁-C₂₄ alkenyl group, a C₁-C₂₄ alkynyl group, a C₁-C₂₄ heteroalkyl group, a C₆-C₂₄ aryl group, a C₆-C₂₄ arylalkyl group, a C₂-C₂₄ heteroaryl group or a C₂-C₂₄ heteroarylalkyl group.

The heteroaryl groups used in the present invention refer to C₂-C₂₄ cyclic aromatic systems including one to three heteroatoms selected from N, O, P, Si, S, Ge, Se, and Te, with the remaining ring atoms being carbon. The rings may be fused together. One or more hydrogen atoms of each heteroaryl group may be substituted with the same substituents as in the aryl groups.

The heteroaromatic rings refer to aromatic hydrocarbon rings in which one or more aromatic carbon atoms are replaced with one or more heteroatoms selected from N, O, P, Si, S, Ge, Se, and Te.

The organic light emitting compound represented by Formula I may be selected from Compounds 1 to 564:

However, it is noted that the scope of Formula I is not limited to Compounds 1 to 564.

The present invention is also directed to an organic light emitting diode including the organic light emitting compound of Formula I. The organic light emitting diode of the present invention includes a first electrode, a second electrode opposite to the first electrode, and an organic layer interposed between the first and second electrodes. The organic layer includes one or more layers selected from a light emitting layer, an electron transport layer, a hole transport layer, an electron injecting layer, a hole injecting layer, a hole blocking layer, and an electron blocking layer. Particularly, the electron transport layer or the electron injecting layer includes the organic light emitting compound of Formula I.

The expression “including the organic light emitting compound” can be interpreted to mean that the organic layer may include the organic light emitting compound of Formula I or two or more different compounds falling within the scope of Formula I.

A more detailed description will be given concerning the organic light emitting diode of the present invention.

The organic light emitting diode of the present invention includes an anode, a hole transport layer, a light emitting layer, an electron transport layer, and a cathode. The organic light emitting diode of the present invention may optionally further include a hole injecting layer and an electron injecting layer. One or more intermediate layers may be further formed in the organic light emitting diode. A hole blocking layer or an electron blocking layer may be further formed in the organic light emitting diode. The diode may further include one or more organic layers with various functions depending on the desired characteristics thereof.

A description will be given concerning a method for fabricating the organic light emitting diode of the present invention. First, an electrode material for the anode is coated on a substrate to form the anode. The substrate may be any of those used in general organic light emitting diodes. The substrate is preferably an organic substrate or a transparent plastic substrate that is excellent in transparency, surface smoothness, ease of handling, and waterproofness. A highly transparent and conductive metal oxide, such as indium tin oxide (ITO), indium zinc oxide (IZO), tin oxide (SnO₂) or zinc oxide (ZnO), is used as the anode material.

A material for the hole injecting layer is coated on the anode by vacuum thermal evaporation or spin coating to form the hole injecting layer. Then, a material for the hole transport layer is coated on the hole injecting layer by vacuum thermal evaporation or spin coating to form the hole transport layer.

The material for the hole injecting layer is not specially limited so long as it is usually used in the art. Example of such materials include 4,4′,4″-tris(2-naphthyl(phenyl)amino)triphenylamine (2-TNATA), N,N′-di(1-naphthyl)-N,N′-diphenylbenzidine) (NPD), N,N′-diphenyl-N,N′-bis(3-methylphenyl)-1,1′-biphenyl-4,4′-diamine (TPD), and N,N′-diphenyl-N,N′-bis[4-(phenyl-m-tolylamino)phenyl]biphenyl-4,4′-diamine (DNTPD).

The material for the hole transport layer is not specially limited so long as it is commonly used in the art. Example of such materials include N,N′-bis(3-methylphenyl)-N,N′-diphenyl-[1,1-biphenyl]-4,4′-diamine (TPD) and N,N′-di(naphthalen-1-yl)-N,N′-diphenylbenzidine (α-NPD).

Subsequently, the organic light emitting layer is laminated on the hole transport layer. A hole blocking layer may be optionally formed on the organic light emitting layer by vacuum thermal evaporation or spin coating. The hole blocking layer blocks holes from entering the cathode through the organic light emitting layer. This role of the hole blocking layer prevents the lifetime and efficiency of the diode from deteriorating. A material having a very low highest occupied molecular orbital (HOMO) energy level is used for the hole blocking layer. The hole blocking material is not particularly limited so long as it has the ability to transport electrons and a higher ionization potential than the light emitting compound. Representative examples of suitable hole blocking materials include BAIq, BCP, and TPBI.

The electron transport layer is deposited on the hole blocking layer by vacuum thermal evaporation or spin coating, and the electron injecting layer is formed thereon. A metal for the cathode is deposited on the electron injecting layer by vacuum thermal evaporation to form the cathode, completing the fabrication of the organic light emitting diode. As the metal for the cathode, there may be used, for example, lithium (Li), magnesium (Mg), aluminum (Al), aluminum-lithium (Al—Li), calcium (Ca), magnesium-indium (Mg—In) or magnesium-silver (Mg—Ag). The organic light emitting diode may be of top emission type. In this case, a transmissive material, such as ITO or IZO, may be used for the cathode.

The material for the electron transport layer functions to stably transport electrons injected from the electron injecting electrode (i.e. the cathode). The organic light emitting compound of Formula I is used as the material for the electron transport layer.

One or more layers selected from the hole injecting layer, the hole transport layer, the electron blocking layer, the light emitting layer, the hole blocking layer, the electron transport layer, and the electron injecting layer may be formed by a monomolecular deposition or solution process. According to the monomolecular deposition process, the material for each layer is evaporated under heat and vacuum or reduced pressure to form the layer in the form of a thin film. According to the solution process, the material for each layer is mixed with a suitable solvent, and then the mixture is formed into a thin film by a suitable method, such as ink-jet printing, roll-to-roll coating, screen printing, spray coating, dip coating or spin coating.

The organic light emitting diode of the present invention can be used in a variety of systems, such as flat panel displays, flexible displays, monochromatic flat panel lighting systems, white flat panel lighting systems, flexible monochromatic lighting systems, and flexible white lighting systems.

The present invention will be explained in more detail with reference to the following specific examples, including synthesis examples for synthesizing dye compounds, and examples and a comparative example for fabricating organic light emitting diodes. However, these examples are provided for illustrative purposes only and are not intended to limit the scope of the invention.

Synthesis Example 1: Synthesis of Compound 1 Synthesis Example 1-1: Synthesis of Intermediate 1-a

25 g (118 mmol) of dibenzofuran-1-boronic acid, 40.5 g (118 mmol) of methyl-5-bromo-2-iodobenzoate, 2.7 g (2.3 mmol) of tetrakis(triphenylphosphine)palladium, 33 g (237 mmol) of potassium carbonate, 200 ml of toluene, 200 ml of 1,4-dioxane, and 100 ml of water were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the reaction mixture was allowed to stand for phase separation. The organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 1-a (33.5 g, yield 74%).

Synthesis Example 1-2: Synthesis of Intermediate 1-b

33.5 g (110 mmol) of Intermediate 1-a was added to 150 ml of tetrahydrofuran in a round bottom flask. After cooling to −10° C., 85 ml (254 mmol) of 3 M methylmagnesium bromide was slowly added dropwise to the flask. The mixture was heated to 40° C., followed by stirring for 4 h. Thereafter, the temperature was lowered to −10° C. 70 ml of 2 N hydrochloric acid was slowly added dropwise to the flask and 70 ml of an aqueous ammonium chloride solution was then added thereto. The temperature was allowed to rise to room temperature. After completion of the reaction, the reaction mixture was washed with water and concentrated under reduced pressure. The resulting residue was purified by column chromatography to give Intermediate 1-b (27 g, yield 80%).

Synthesis Example 1-3: Synthesis of Intermediate 1-c

27 g (89.2 mmol) of Intermediate 1-b and 70 ml of phosphoric acid were placed in a round bottom flask under a nitrogen atmosphere. The mixture was stirred at room temperature for 12 h. After completion of the reaction, the reaction mixture was extracted and concentrated. The resulting residue was purified by column chromatography to give Intermediate 1-c (17.6 g, yield 70%).

Synthesis Example 1-4: Synthesis of Intermediate 1-d

17.6 g (48.4 mmol) of Intermediate 1-c was placed in a round bottom flask and 200 ml of tetrahydrofuran was then added thereto under a nitrogen atmosphere. After cooling to −78° C., 36.3 ml (58.1 mmol) of 1.6 M butyllithium was slowly added dropwise to the flask. 1 h after the addition, 7.0 ml (62.9 mmol) of trimethyl borate was slowly added to the flask while maintaining the same temperature. Thereafter, the resulting mixture was stirred at room temperature. After completion of the reaction, the organic layer was concentrated under reduced pressure and recrystallized from hexane to give Intermediate 1-d (13 g, yield 82%).

Synthesis Example 1-5: Synthesis of Compound 1

5 g (15.2 mmol) of Intermediate 1-d, 6.5 g (16.7 mmol) of 2-chloro-4,6-diphenyl-1,3,5-triazine, 0.3 g (0.3 mmol) of tetrakis(triphenylphosphine)palladium, 4.2 g (30.4 mmol) of potassium carbonate, 25 ml of toluene, 25 ml of 1,4-dioxane, and 15 ml of water were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Compound 1 (6.8 g, yield 76%).

MS (MALDI-TOF): m/z 515.20 [M]⁺

Synthesis Example 2: Synthesis of Compound 5 Synthesis Example 2-1: Synthesis of Intermediate 2-a

Intermediate 2-a (yield 42%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2,4-dichloro-6-phenyl-1,3,5-triazine and 1-naphthaleneboronic acid were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

Synthesis Example 2-2: Synthesis of Compound 5

Compound 5 (yield 72%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 2-a was used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine.

MS (MALDI-TOF): m/z 565.22 [M]⁺

Synthesis Example 3: Synthesis of Compound 71 Synthesis Example 3-1: Synthesis of Intermediate 3-a

50 g (183 mmol) of 2-bromo-9,9-dimethylfluorene, 59.3 g (1098 mmol) of an aqueous sodium methoxide solution, 10.4 g (54.9 mmol) of copper iodide, and 200 ml of methanol were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-a (33.2 g, yield 81%).

Synthesis Example 3-2: Synthesis of Intermediate 3-b

30 g (133 mmol) of Intermediate 3-a, 23.8 g (133 mmol) of N-bromosuccinimide, and 600 ml of dimethylformamide were placed in a round bottom flask under a nitrogen atmosphere. The mixture was stirred at 50° C. for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-b (28 g, yield 70%).

Synthesis Example 3-3: Synthesis of Intermediate 3-c

Intermediate 3-c (yield 77%) was synthesized in the same manner as in Synthesis Example 1-4, except that Intermediate 3-b was used instead of Intermediate 1-c.

Synthesis Example 3-4: Synthesis of Intermediate 3-d

Intermediate 3-d (yield 52%) was synthesized in the same manner as in Synthesis Example 1-5, except that 1-bromo-3-chloro-2-fluorobenzene and Intermediate 3-c were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

Synthesis Example 3-5: Synthesis of Intermediate 3-e

30 g (85 mmol) of Intermediate 3-d and 300 ml of dichloromethane were placed in a round bottom flask under a nitrogen atmosphere. After cooling to 0° C., a dilute solution of 63.9 g (255 mmol) of boron tribromide in 150 ml of dichloromethane was slowly added dropwise to the flask. The temperature was allowed to rise to room temperature. The mixture was stirred for 6 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-e (21.3 g, yield 74%).

Synthesis Example 3-6: Synthesis of Intermediate 3-f

20 g (59 mmol) of Intermediate 3-e, 13 g (94.5 mmol) of potassium carbonate, and 200 ml of 1-methyl-2-pyrrolidinone were placed in a round bottom flask under a nitrogen atmosphere. The mixture was stirred at 150° C. for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-f (13.5 g, yield 72%).

Synthesis Example 3-7: Synthesis of Intermediate 3-q

13 g (40.8 mmol) of Intermediate 3-f, 12.4 g (48.9 mmol) of bis(pinacolato)diborane, 2 g (2.4 mmol) of tris(dibenzylideneacetone)palladium, 11.6 g (122 mmol) of potassium acetate, 2.7 g (9.8 mmol) of tricyclohexylphosphine, and 150 ml of N-dimethylformamide were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 3-g (10.8 g, yield 65%).

Synthesis Example 3-8: Synthesis of Compound 71

Compound 71 (yield 69%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 3-g was used instead of Intermediate 1-d.

MS (MALDI-TOF): m/z 515.20 [M]⁺

Synthesis Example 4: Synthesis of Compound 72 Synthesis Example 4-1: Synthesis of Compound 72

Compound 72 (yield 46%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(3-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 3-g were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 591.23 [M]⁺

Synthesis Example 5: Synthesis of Compound 164 Synthesis Example 5-1: Synthesis of Intermediate 5-a

Intermediate 5-a (yield 76%) was synthesized in the same manner as in Synthesis Example 1-5, except that 3-bromodibenzofuran and phenylboronic acid were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

Synthesis Example 5-2: Synthesis of Intermediate 5-b

50 g (204 mmol) of Intermediate 5-a and 500 ml of tetrahydrofuran were placed in a round bottom flask under a nitrogen atmosphere. After cooling to −78° C., 128 ml (204 mmol) of 1.6 M butyllithium was slowly added dropwise to the flask. The mixture was stirred for 1 h. To the mixture slowly added dropwise 14.3 g (245 mmol) of acetone. The resulting mixture was stirred at room temperature for 6 h. After completion of the reaction, 50 ml of an aqueous ammonium chloride solution was added for phase separation. The organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 5-b (38.3 g, yield 62%).

Synthesis Example 5-3: Synthesis of Intermediate 5-c

Intermediate 5-c (yield 69%) was synthesized in the same manner as in Synthesis Example 1-3, except that Intermediate 5-b was used instead of Intermediate 1-b.

Synthesis Example 5-4: Synthesis of Intermediate 5-d

14.5 g (50.9 mmol) of Intermediate 5-c and 150 ml of dichloromethane were stirred in a 1 L reactor. To the mixture was slowly added dropwise 8.9 g (56 mmol) at room temperature. The resulting mixture was stirred for 5 h. After completion of the reaction, the reaction mixture was precipitated by adding methanol. Filtration of the precipitate gave Intermediate 5-d (9.4 g, yield 51%).

Synthesis Example 5-5: Synthesis of Intermediate 5-e

Intermediate 5-e (yield 65%) was synthesized in the same manner as in Synthesis Example 1-4, except that Intermediate 5-d was used instead of Intermediate 1-c.

Synthesis Example 5-6: Synthesis of Compound 164

Compound 164 (yield 73%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 5-e was used instead of Intermediate 1-d.

MS (MALDI-TOF): m/z 515.20 [M]⁺

Synthesis Example 6: Synthesis of Compound 167 Synthesis Example 6-1: Synthesis of Compound 167

Compound 167 (yield 48%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 5-e were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 591.23 [M]⁺

Synthesis Example 7: Synthesis of Compound 197 Synthesis Example 7-1: Synthesis of Intermediate 7-a

Intermediate 7-a (yield 66%) was synthesized in the same manner as in Synthesis Examples 1-1 to 1-4, except that dibenzofuran-3-boronic acid and methyl-5-bromo-1-iodobenzoate were used instead of dibenzofuran-1-boronic acid and methyl-5-bromo-2-iodobenzoate in Synthesis Example 1-1, respectively.

Synthesis Example 7-2: Synthesis of Compound 197

Compound 197 (yield 63%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 7-a was used instead of Intermediate 1-d.

MS (MALDI-TOF): m/z 515.20 [M]⁺

Synthesis Example 8: Synthesis of Compound 200 Synthesis Example 8-1: Synthesis of Compound 200

Compound 200 (yield 68%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 7-a were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 591.23 [M]⁺

Synthesis Example 9: Synthesis of Compound 233 Synthesis Example 9-1: Synthesis of Intermediate 9-a

50 g (202 mmol) of 3-bromodibenzofuran, 54.6 g (1214 mmol) of an aqueous sodium methoxide solution, 11.5 g (60.7 mmol) of copper iodide, and 200 ml of methanol were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-a (36 g, yield 90%).

Synthesis Example 9-2: Synthesis of Intermediate 9-b

36 g (181 mmol) of Intermediate 9-a, 32.3 g (181 mmol) of N-bromosuccinimide, and 700 ml of dimethylformamide were placed in a round bottom flask under a nitrogen atmosphere. The mixture was stirred at 50° C. for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-b (35 g, yield 70%).

Synthesis Example 9-3: Synthesis of Intermediate 9-c

Intermediate 9-c (yield 71%) was synthesized in the same manner as in Synthesis Example 1-4, except that Intermediate 9-b was used instead of Intermediate 1-c.

Synthesis Example 9-4: Synthesis of Intermediate 9-d

Intermediate 9-d (yield 64%) was synthesized in the same manner as in Synthesis Example 1-5, except that methyl-2-bromobenzoate and Intermediate 9-c were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

Synthesis Example 9-5: Synthesis of Intermediate 9-e

Intermediate 9-e (yield 77%) was synthesized in the same manner as in Synthesis Example 1-2, except that Intermediate 9-d was used instead of Intermediate 1-a.

Synthesis Example 9-6: Synthesis of Intermediate 9-f

Intermediate 9-f was synthesized in a yield of 67% in the same manner as in Synthesis Example 1-3, except that Intermediate 9-e was used instead of Intermediate 1-b.

Synthesis Example 9-7: Synthesis of Intermediate 9-q

30 g (95.4 mmol) of Intermediate 9-f and 200 ml of dichloromethane were placed in a round bottom flask under a nitrogen atmosphere. The temperature was lowered to 0° C. A dilute solution of 120 g (143 mmol) of boron tribromide in 300 ml of dichloromethane was slowly added dropwise to the flask. The mixture was stirred at room temperature for 3 h. After completion of the reaction, the reaction solution was added to 1 L of distilled water. The organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-g (19.2 g, yield 67%).

Synthesis Example 9-8: Synthesis of Intermediate 9-h

10 g (33.2 mmol) of Intermediate 9-g was placed in a round bottom flask under a nitrogen atmosphere. The temperature was lowered to 0° C. 3.2 ml (39.9 mmol) of pyridine and 7.3 ml (43.2 mmol) of trifluoromethanesulfonic anhydride were slowly added dropwise to the flask. The mixture was stirred at room temperature for 2 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-h (12.2 g, yield 85%).

Synthesis Example 9-9: Synthesis of Intermediate 9-i

8.5 g (26.7 mmol) of Intermediate 9-h, 8.8 g (34.7 mmol) of bis(pinacolato)diborane, 1 g (1.3 mmol) of (diphenylphosphinoferrocene)palladium dichloride, 7.6 g (80 mmol) of potassium acetate, and 90 ml of toluene were placed in a round bottom flask under a nitrogen atmosphere. The mixture was refluxed for 12 h. After completion of the reaction, the organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 9-i (8 g, yield 75%).

Synthesis Example 9-10: Synthesis of Compound 233

Compound 233 (yield 78%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 9-i was used instead of Intermediate 1-d.

MS (MALDI-TOF): m/z 515.20 [M]⁺

Synthesis Example 10: Synthesis of Compound 234 Synthesis Example 10-1: Synthesis of Compound 234

Compound 234 (yield 52%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(3-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 9-i were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 591.23 [M]⁺

Synthesis Example 11: Synthesis of Compound 293 Synthesis Example 11-1: Synthesis of Intermediate 11-a

37 g (156 mmol) of (3-amino-benzofuran-2-yl)-phenylmethanone, 16.9 g (281 mmol) of urea, and 185 mL of acetic acid were placed in a 500 mL reactor. The mixture was refluxed with stirring for 12 h. After completion of the reaction, the reaction mixture was precipitated by adding excess water. The precipitate was collected by filtration, slurried with hot methanol, filtered, slurried with hot toluene, filtered, and dried to obtain Intermediate 11-a (24 g, yield 59%).

Synthesis Example 11-2: Synthesis of Intermediate 11-b

15 g (44 mmol) of Intermediate 11-a and 150 mL of phosphorus oxychloride were placed in a 500 mL reactor. The mixture was refluxed with stirring for 3 h. After completion of the reaction, the reaction mixture was precipitated by slowly adding excess water at 0° C. The precipitate was collected by filtration and purified by column chromatography to give 21 g (yield 81%) of Intermediate 11-b.

Synthesis Example 11-3: Synthesis of Compound 293

Compound 293 (yield 57%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 11-b and Intermediate 5-e were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 528.18 [M]⁺

Synthesis Example 12: Synthesis of Compound 313 Synthesis Example 12-1: Synthesis of Intermediate 12-a

27.4 g (232 mmol) of 2-aminobenzonitrile and 300 mL of tetrahydrofuran were stirred in a 1 L reactor. After cooling to 0° C., 88.2 mL (487 mmol) of 3 M phenylmagnesium bromide was added dropwise to the flask. The mixture was refluxed for 3 h. After cooling to 0° C., a solution of 44.3 g (732 mmol) of ethyl chloroformate in 200 mL of tetrahydrofuran was added dropwise to the reaction mixture. The resulting mixture was refluxed for 2 h. After cooling to 0° C., to the reaction mixture was added a saturated aqueous solution of ammonium chloride. The organic layer was extracted and concentrated under reduced pressure. The resulting residue was purified by column chromatography to give Intermediate 12-a (40 g, yield 78%).

Synthesis Example 12-2: Synthesis of Intermediate 12-b

40 g (181 mmol) of Intermediate 12-a and 400 mL of phosphorus oxychloride were placed in a 1 L reactor. The mixture was refluxed for 5 h. After cooling to 0° C., distilled water was added dropwise to the reactor. The reaction mixture was filtered and the resulting residue was purified by column chromatography to give Intermediate 12-b (29.5 g, yield 68%).

Synthesis Example 12-3: Synthesis of Compound 313

Compound 313 (yield 54%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 12-b and Intermediate 3-g were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 488.19 [M]⁺

Synthesis Example 13: Synthesis of Compound 329 Synthesis Example 13-1: Synthesis of Intermediate 13-a

90 g (676 mmol) of 2-hydroxyphenylacetonitrile, 68.8 g (338 mmol) of 4-dimethylaminopyridine, 137 g (1352 mmol) of triethylamine, and 900 mL of methylene chloride were placed in a 2 L reactor and 82.4 g (676 mmol) of benzoyl chloride was then added dropwise thereto at 0° C. Thereafter, the mixture was stirred at room temperature for 4 h. After completion of the reaction, the reaction mixture was concentrated and the resulting residue was purified by column chromatography to give Intermediate 13-a (40 g, yield 61%).

Synthesis Example 13-2: Synthesis of Intermediate 13-b

40 g (169 mmol) of Intermediate 13-a, 9.5 g (34 mmol) of tricyclohexylphosphine, 1.9 g (17 mmol) of zinc, 3.8 g (17 mmol) of palladium acetate, and 400 mL of dimethylformamide were placed in a 1 L reactor. The mixture was refluxed with stirring under a nitrogen atmosphere for 12 h. After completion of the reaction, the reaction mixture was added to excess water at room temperature. The resulting brown crystal was collected by filtration and purified by column chromatography to give Intermediate 13-b (20 g, yield 52%).

Synthesis Example 13-3: Synthesis of Intermediate 13-c

Intermediate 13-c (10 g, yield 62%) was synthesized in the same manner as in Synthesis Example 11-1, except that Intermediate 13-b was used instead of (3-amino-benzofuran-2-yl)-phenylmethanone.

Synthesis Example 13-4: Synthesis of Intermediate 13-d

Intermediate 13-d (yield 77%) was synthesized in the same manner as in Synthesis Example 11-2, except that Intermediate 13-c was used instead of Intermediate 11-a.

Synthesis Example 13-6: Synthesis of Compound 329

Compound 329 (yield 54%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 13-d was used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine.

MS (MALDI-TOF): m/z 528.18 [M]⁺

Synthesis Example 14: Synthesis of Compound 341 Synthesis Example 14-1: Synthesis of Compound 341

Compound 341 (yield 58%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 12-b and Intermediate 9-i were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 488.19 [M]⁺

Synthesis Example 15: Synthesis of Compound 370 Synthesis Example 15-1: Synthesis of Intermediate 15-a

Ethyl cyanoacetate (139.8 g, 1.236 mol), potassium cyanide (29.5 g, 0.453 mol), and potassium hydroxide (46.2 g, 0.824 mol) were dissolved in 920 mL of dimethylformamide in a 2 L round bottom flask under a nitrogen atmosphere. The solution was stirred at 10° C. for 20 min. Thereafter, the solution was added with 1-nitronaphthalene (92 g, 531 mol), followed by stirring at 60° C. for 4 h. After completion of the reaction, the reaction mixture was concentrated and 600 mL of a 10% aqueous sodium hydroxide solution was added thereto. The resulting mixture was refluxed with stirring. The solid was collected by filtration and purified by column chromatography to give Intermediate 15-a (50 g, yield 56%).

Synthesis Example 15-2: Synthesis of Intermediate 15-b

Intermediate 15-a (20.0 g, 169 mmol) and tetrahydrofuran (200 mL) were placed in a 1 L round bottom flask filled with nitrogen and 3 M phenylmagnesium bromide (113 mL, 623 mmol) was slowly added dropwise thereto at 0° C. The mixture was refluxed with stirring for 3 h. When the starting material disappeared, the temperature was again lowered. A solution of 3-bromobenzoyl chloride (44.58 g, 0.203 mmol) in 200 mL of tetrahydrofuran was slowly added dropwise to the flask. The resulting mixture was refluxed with stirring for 2 h. The reaction was quenched with an aqueous ammonium chloride solution. The reaction mixture was extracted with ethyl acetate and water. The organic layer was concentrated under reduced pressure and the resulting residue was purified by column chromatography to give Intermediate 15-b (37 g, yield 30%).

Synthesis Example 15-3: Synthesis of Compound 370

Compound 370 (yield 57%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 15-b and Intermediate 7-a were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 614.24 [M]⁺

Synthesis Example 16: Synthesis of Compound 375 Synthesis Example 16-1: Synthesis of Intermediate 16-a

Intermediate 16-a (yield 42%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2,4-dichloro-6-phenyl-1,3,5-triazine and benzofuran-1-boronic acid were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

Synthesis Example 16-2: Synthesis of Intermediate 16-b

Intermediate 16-b (yield 55%) was synthesized in the same manner as in Synthesis Examples 1-2 to 1-4, except that 3 M ethylmagnesium bromide was used instead of 3 M methylmagnesium bromide in Synthesis Example 1-2.

Synthesis Example 16-3: Synthesis of Compound 375

Compound 375 (yield 55%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 16-a and Intermediate 16-b were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 633.24 [M]⁺

Synthesis Example 17: Synthesis of Compound 414 Synthesis Example 17-1: Synthesis of Intermediate 17-a

Intermediate 17-a (yield 57%) was synthesized in the same manner as in Synthesis Examples 3-1 to 3-7, except that 2-bromo-9,9-diethylfluorene was used instead of 2-bromo-9,9-dimethylfluorene in Synthesis Example 3-1.

Synthesis Example 17-2: Synthesis of Compound 414

Compound 414 (yield 54%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 12-b and Intermediate 17-a were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 516.22 [M]⁺

Synthesis Example 18: Synthesis of Compound 443 Synthesis Example 18-1: Synthesis of Intermediate 18-a

Intermediate 18-a (yield 52%) was synthesized in the same manner as in Synthesis Examples 5-2 to 5-5, except that 2,4-dimethyl-3-pentanone was used instead of acetone in Synthesis Example 5-2.

Synthesis Example 18-2: Synthesis of Compound 443

Compound 443 (yield 55%) was synthesized in the same manner as in Synthesis Example 1-5, except that 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine and Intermediate 18-a were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 647.29 [M]⁺

Synthesis Example 19: Synthesis of Compound 474 Synthesis Example 19-1: Synthesis of Intermediate 19-a

Intermediate 19-a (yield 55%) was synthesized in the same manner as in Synthesis Examples 1-2 and 1-3, except that 3 M ethylmagnesium bromide and Intermediate 9-d were used instead of 3 M methylmagnesium bromide and Intermediate 1-a in Synthesis Example 1-2, respectively.

Synthesis Example 19-2: Synthesis of Intermediate 19-b

Intermediate 19-b (yield 67%) was synthesized in the same manner as in Synthesis Examples 9-7 to 9-9, except that Intermediate 19-a was used instead of Intermediate 9-f in Synthesis Example 9-7.

Synthesis Example 19-2: Synthesis of Compound 474

Compound 474 (yield 60%) was synthesized in the same manner as in Synthesis Example 1-5, except that Intermediate 11-b and Intermediate 19-b were used instead of 2-chloro-4,6-diphenyl-1,3,5-triazine and Intermediate 1-d, respectively.

MS (MALDI-TOF): m/z 556.22 [M]⁺

Examples 1 to 19: Fabrication of Organic Light Emitting Diodes

ITO glass was patterned to have a light emitting area of 2 mm×2 mm, followed by cleaning. After the cleaned ITO glass was mounted in a vacuum chamber, the base pressure was adjusted to 1×10⁻⁶ torr. HATCN (50 Å), NPD (650 Å), [BH]+ Blue dopant (BD) 5% (200 Å), the corresponding compound shown in Table 1 (300 Å), Liq (10 Å), and Al (1,000 Å) were deposited in this order on the ITO glass to fabricate an organic light emitting diode. The luminescent properties of the organic light emitting diode were measured at 0.4 mA.

The structures of HATCN, NPD, BD, BH, and Liq are as follows:

Comparative Example 1

An organic light emitting diode was fabricated in the same manner as in Examples 1-19, except that ET was used instead of the compounds shown in Table 1. ET is widely used as an electron transport material and its structure is as follows.

The organic electroluminescence diodes fabricated in Examples 1-19 and Comparative Example 1 were measured for voltage, luminance, color coordinates, and lifetime. The results are shown in Table 1. T₉₅ indicates the time at which the luminance of each diode was decreased to 95% of the initial luminance (2000 cd/m²).

TABLE 1 Properties ETL V Cd/A CIEx CIEy T₉₅ (Hrs) Comparative ET 4.2 6.4 0.133 0.129 16 Example 1 Example 1 Compound 1 3.6 8.0 0.132 0.130 35 Example 2 Compound 5 3.6 7.9 0.133 0.128 43 Example 3 Compound 71 3.4 8.0 0.132 0.126 40 Example 4 Compound 72 3.8 7.9 0.133 0.125 36 Example 5 Compound 164 3.3 7.6 0.132 0.126 34 Example 6 Compound 167 3.9 7.6 0.133 0.125 45 Example 7 Compound 197 4.0 7.5 0.133 0.125 42 Example 8 Compound 200 3.6 8.1 0.132 0.130 37 Example 9 Compound 233 3.4 8.0 0.133 0.128 37 Example 10 Compound 234 3.6 7.8 0.133 0.127 34 Example 11 Compound 293 3.6 8.0 0.132 0.130 45 Example 12 Compound 313 3.6 7.9 0.133 0.128 42 Example 13 Compound 329 3.4 8.0 0.132 0.126 40 Example 14 Compound 341 3.8 7.9 0.133 0.125 34 Example 15 Compound 370 3.3 8.0 0.132 0.126 38 Example 16 Compound 375 3.9 7.9 0.133 0.125 40 Example 17 Compound 414 4.0 7.6 0.132 0.126 33 Example 18 Compound 443 3.6 7.6 0.133 0.125 37 Example 19 Compound 474 3.7 7.5 0.133 0.125 41

As can be seen from the results in Table 1, the inventive organic compounds had higher efficiencies, lower driving voltages, and longer lifetimes than ET, which is widely used as an electron transport material. Therefore, it can be concluded that the inventive compounds are suitable for the fabrication of organic light emitting diodes with improved characteristics. 

What is claimed is:
 1. An organic light emitting compound represented by Formula I: HAr₁-(L)_(n)-HAr₂  (I) wherein L represents a linker and is a single bond or is selected from substituted or unsubstituted C₁-C₃₀ alkylene groups, substituted or unsubstituted C₂-C₃₀ alkenylene groups, substituted or unsubstituted C₂-C₃₀ alkynylene groups, substituted or unsubstituted C₃-C₃₀ cycloalkylene groups, substituted or unsubstituted C₂-C₃₀ heterocycloalkylene groups, substituted or unsubstituted C₆-C₃₀ arylene groups, and substituted or unsubstituted C₂-C₃₀ heteroarylene groups, n is an integer from 1 to 3, provided that when n is equal to or greater than 2, the plurality of L groups are identical to or different from each other; wherein HAr₁ is a substituted or unsubstituted C₆-C₃₀ aryl group or a substituted or unsubstituted C₂-C₃₀ heteroaryl group; and wherein HAr₂ is selected from the following structures A to E:

where X₁ is CR₁₁ or N, X₂ is CR₁₂ or N, X₃ is CR₁₃ or N, X₄ is CR₁₄ or N, X₅ is CR₁₅ or N, X₆ is CR₁₆ or N, X₇ is CR₁₇ or N, X₈ is CR₁₈ or N, X₉ is CR₁₉ or N, and X₁₀ is CR₂₀ or N, with the proviso that at least two of X₁ to X₄ are selected from CR₁₁ to CR₁₄, at least three of X₅ to X₁₀ are selected from CR₁₅ to CR₂₀, and one of X₁ to X₁₀ is a carbon atom linked to L, where R₁ and R₂ are identical to or different from each other and are each independently selected from a hydrogen atom, a deuterium atom, substituted or unsubstituted C₁-C₃₀ alkyl groups, substituted or unsubstituted C₂-C₃₀ alkenyl groups, substituted or unsubstituted C₂-C₃₀ alkynyl groups, substituted or unsubstituted C₁-C₃₀ alkoxy groups, substituted or unsubstituted C₁-C₃₀ alkylthioxy groups, substituted or unsubstituted C₁-C₃₀ alkylamine groups, substituted or unsubstituted C₁-C₂₄ alkylsilyl groups, an amino group, a thiol group, a cyano group, a hydroxyl group, a nitro group, and halogen groups, and where R₁₁ to R₂₀ are identical to or different from each other and are each independently selected from a hydrogen atom, a deuterium atom, substituted or unsubstituted C₁-C₃₀ alkyl groups, substituted or unsubstituted C₂-C₃₀ alkenyl groups, substituted or unsubstituted C₂-C₃₀ alkynyl groups, substituted or unsubstituted C₃-C₃₀ cycloalkyl groups, substituted or unsubstituted C₂-C₃₀ heterocycloalkyl groups, substituted or unsubstituted C₅-C₃₀ cycloalkenyl groups, substituted or unsubstituted C₁-C₃₀ alkoxy groups, substituted or unsubstituted C₆-C₃₀ aryloxy groups, substituted or unsubstituted C₁-C₃₀ alkylthioxy groups, substituted or unsubstituted C₆-C₃₀ arylthioxy groups, substituted or unsubstituted C₁-C₃₀ alkylamine groups, substituted or unsubstituted C₆-C₃₀ arylamine groups, substituted or unsubstituted C₆-C₅₀ aryl groups, substituted or unsubstituted C₂-C₅₀ heteroaryl groups containing O, N or S as a heteroatom, substituted or unsubstituted C₁-C₂₄ alkylsilyl groups, substituted or unsubstituted C₆-C₂₄ arylsilyl groups, an amino group, a thiol group, a cyano group, a hydroxyl group, a nitro group, and halogen groups.
 2. The organic light emitting compound according to claim 1, wherein the “substituted” in the definition of “substituted or unsubstituted” indicates substitution with at least one substituent selected from the group consisting of deuterium, a cyano group, halogen groups, a hydroxyl group, a nitro group, C₁-C₂₄ alkyl groups, C₁-C₂₄ halogenated alkyl groups, C₂-C₂₄ alkenyl groups, C₂-C₂₄ alkynyl groups, C₁-C₂₄ heteroalkyl groups, C₆-C₂₄ aryl groups, C₇-C₂₄ arylalkyl groups, C₂-C₂₄ heteroaryl groups, C₂-C₂₄ heteroarylalkyl groups, C₁-C₂₄ alkoxy groups, C₁-C₂₄ alkylamino groups, C₁-C₂₄ arylamino groups, C₁-C₂₄ heteroarylamino groups, C₁-C₂₄ alkylsilyl groups, C₆-C₂₄ arylsilyl groups, and C₆-C₂₄ aryloxy groups.
 3. The organic light emitting compound according to claim 1, wherein HAr₁ is selected from the following structures E1 to E33:

wherein Z₁ to Z₈ are identical to or different from each other and each independently have the same meanings as R₁, R₂, and R₁₁ to R₂₀, and each of Z₁ to Z₈ and substituents thereof optionally forms an aliphatic, aromatic, heteroaliphatic or heteroaromatic fused ring with the adjacent group.
 4. An organic light emitting diode comprising a first electrode, a second electrode opposite to the first electrode, and an organic layer interposed between the first and second electrodes wherein the organic layer comprises the compound represented by Formula I according to claim
 1. 5. The organic light emitting diode according to claim 5, wherein the organic layer comprises one or more layers selected from a light emitting layer, an electron transport layer, a hole transport layer, an electron injecting layer, a hole injecting layer, a hole blocking layer, and an electron blocking layer.
 6. The organic light emitting diode according to claim 6, wherein the electron transport layer or the electron injecting layer comprises the compound represented by Formula I. 